Date published: 2025-12-19

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2-(5-ethyl-2-thienyl)quinoline-4-carbonyl chloride

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Molecular Weight:
301.80
Molecular Formula:
C16H12ClNOS
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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2-(5-ethyl-2-thienyl)quinoline-4-carbonyl chloride functions as a reagent in organic synthesis in the formation of various quinoline derivatives. 2-(5-ethyl-2-thienyl)quinoline-4-carbonyl chloride involves the acylation of amines and other nucleophiles, leading to the formation of quinoline-4-carbonyl compounds. 2-(5-ethyl-2-thienyl)quinoline-4-carbonyl chloride participates in Friedel-Crafts acylation reactions, where it acts as an acyl chloride, reacting with the aromatic ring of the quinoline substrate. The resulting product can then be further modified to create diverse molecular structures for potential use in various research applications. This compound′s role in the synthesis of quinoline derivatives makes it valuable for the development of new materials and compounds in the field of organic chemistry.

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

2-(5-ethyl-2-thienyl)quinoline-4-carbonyl chloride, 100 mg

sc-320978
100 mg
$153.00